Organic phosphorus compounds



United States Patent 3,269,812 ORGANIC PHOSPHORUS COMPOUNDS Riyad R. lrani, Florissant, and Kurt Moedritzer, Webster Grove, Mo., assignors to Monsanto Company, a corporation of Delaware No Drawing. Original application Dec. 3, 1962, Ser. No. 241,562. Divided and this application Aug. 27, 1965, Ser. No. 493,300

6 Claims. (Cl. 44-72) This application is a continuation-in-part of applications, SN. 152,048, filed November 13, 1961, and SN. 217,276, filed August 16, 1962, and is a divisional application of application S.N. 241,562, filed December '3, 1962.

This invention relates to organic compounds of phosphorus.

An object of this invention is to provide new and useful organic compounds of phosphorus containing a PCN0P linkage in their molecules.

A further object of this invention is to provide new and useful organic compounds of phosphorus containing a C 3 POI\]ICP linkage in their molecules with the C 3 group being a hydrophobic and/or lipophilic group.

A further object of this invention is to provide new and useful organophosphonic acids, as well as their salts and esters.

A more specific object of this invention is to provide new and useful organo-amino-di-alkylene phosphonic acids or the salts thereof which exhibit, among other things, combined surfactancy and de fiocculating properties.

A more specific object of this invention is to provide new and useful organo-amino-di-alkylene phosphonate esters which exhibit, among other things, the unique abil ity of solubilizing water in water-immiscible solvents.

Other objects of this invention will appear from the description hereinafter.

This invention is directed to new and useful organoamino-di-alkylenephosphonic acid compounds, as well as the salts and esters thereof, said compounds having the general formula wherein: R is selected from the class consisting of aliphatic hydrocarbyl, alicyclic, aryl, alkaryl, aralkyl and heterocyclic groups of from 4 to 30 carbon atoms; R R R and R are selected from the class consisting of hydrogen, aliphatic hydrocarbyl, alicyclic, aryl, alkaryl, aralkyl and heterocyclic groups of from 1 to 30 carbon atoms; and X is selected from the class consisting of cations, alkyl groups of from 1 to 30 carbon atoms, aryl groups, and alkaryl groups. By the term cations is meant hydrogen ions, alkali metal cations, alkaline earth metal cations, ammonium ions, or amine ions. For the above-mentioned groups which represent R, R R R R and X when it represents alkyl, aryl and alkaryl groups, the OH, COOH, OCH halogen, N0 and S0 substituted derivatives of the groups are intended to be also included within their meaning. However, for most end use applications the compounds of the instant invention should preferably contain not more than 25 carbon atoms associated with R, R R R R and X when it repreice sents alkyl, aryl, and aralkyl groups, and there are few, if any, end uses, in which the foregoing groups contain more than a total of 50 carbon atoms.

These compounds can be characterized quite generally as having a PCNC-P linkage in their molecules and are generically described in this specification by the general terms organo-amino-di-alkylene-phosphonic acids, the salts of organo-amino-di-alkylenephosphonic acids, and the esters of organo-amino-di-alkylenephosphonic acid.

The compounds of the invention can be prepared by various methods with the following methods presented as being representative for their preparation.

The organo-arnino-di-alkylenephosphonic acids can be prepared by the reaction of primary amines, a compound containing a carbonyl group, such as an aldehyde, or ketone, and orthophosphorous acid. Generally, by heating the mixture above 50 C. at a low pH, preferably around pH 2 or below, the extent of the reaction is usually completed in one to three hours. Another method is the hydrolysis of the ester, i.e., tetraalkyl organo-aminodi-alkylenephosphonate, with concentrated \I-ICl or HBr. Generally by refluxing the ester and acid at reflux temperature for a period usually about three hours is all that is required for the hydrolysis. In the foregoing reactions molar ratios should be used in proportions which will form the desired P-CNCP molecular linkage.

The salts of organo-amino-di-alkylene phosphonic acids can be prepared by neutralization of the acids with a stoichiometric amount of a base that contains essentially the desired cation. Bases such as those containing an alkali metal, alkaline earth, ammonia and amines are especially suited. For example, to make a sodium salt, one of the organo-amino-di-alkylene phosphonic acids can be neutralized with a stoichiometric amount of a base containing the sodium cation, such as NaOI-I, NagCO and the like.

The esters of organo-amino-di-alkylene-phosphonic acids can be prepared directly by the reaction of primary amines, a compound containing a carbonyl group, such as an aldehyde or ketone, and a dialkyl phosphonate. Generally by heating the mixture above 50 C. the extent of the reaction is usually completed in about one to three hours. In some cases it is advantageous to form a reaction product of an aldimine or ketimine with a dialkyl phosphonate and still further react the product with a mixture of an aldehyde or ketone and dialkyl phosphonate. This method can result in forming a C- substituted P-C-N-CP molecular linkage. It should be noted that here also it is necessary to use the correct molar ratios in order to obtain satisfactory yields with the desired PCNCP molecular linkage.

For the foregoing methods of preparation reaction conditions such as temperature, pH, and time for reaction can be varied with the optimum conditions for the reac tions readily ascertained by those skilled in the art. Reference to the specific examples presented hereinafter may be of aid in order to further assist in teaching the methods of their preparation.

The following examples are presented to illustrate the invention, with parts by weight being used in the examples unless indicated otherwise.

EXAMPLE I Into a conventional jacketed, glass-lined mixing vessel fitted with a water condenser are charged 164 parts of orthophosphorous acid, 102 parts of n-hexylamine, and 50 parts of water. The resulting mixture is stirred continuously through the remainder of the process described below. The mixture is heated to C., and maintained at about 95 C. while, over a period of about 20 minutes, 66 parts (10% excess) of paraformalde-hyde are added slowly thereinto. Then, for an additional hour after all the formaldehyde has been added, the resulting mixture is refluxed at a temperature of about 110 C. after which time the reaction mixture is cooled to room temperature. By nuclear magnetic resonance measurements, it is found that more than 90% of the orthophosphorous acid has been converted to the desired product, hexylaminodi- (methylphosphonic acid), C H N(CH PO(OH) The equivalent weight of this product, by titration, is found to be about 96.1, which compares excellently with the calculated value of about 96.3.

EXAMPLE II Into a mixing vessel similar to that described in Example I, above, are charged 134 parts of cyclohexylamine hydrochloride, 164 parts of orthophosphorous acid and 25 parts of water. The resulting mixture is blended together and heated to 100 C. Then, over a period of about 30 minutes, 66 parts excess) of paraformaldehyde are added slowly thereinto. Then for an additional hour after all of the formaldehyde has been added the resulting mixture is refluxed at a temperature of about 110 C. after which the reaction mixture is cooled to room temperature. By nuclear magnetic resonance measurements, it is found that more than 90% of the orthophosphorous acid has been converted to the desired product, cyclohexylaminodi(methylphosphonic acid),

The equivalent weight of this product, by titration, is found to be about 96.6, which compares excellently with the calculated value of about 95.7.

EXAMPLE III Into a mixing vessel such as that described in Example I, above, are charged 164 parts of orthophosphorous acid, 213 parts of n-tetradecylamine, and 50 parts of water. The resulting mixture is stirred continuously through the remainder of the process described below. The mixture is heated to 95 C., and maintained at about 95 C. while, over a period of about 20 minutes, 66 parts (10% excess) of paraformaldehyde are added slowly thereinto. Then for an additional hour after all the formaldehyde has been added, the resulting mixture is refluxed at a temperature of about 110 C. after which the reaction mixture is cooled to room temperature. By nuclear magnetic resonance measurements, it is found that more than 90% of the orthophosphorous acid has been converted to the desired product, n-tetradecylamino-di-(methylphosphonic acid), C H N(CH PO(OH) The equivalent weight of this product, by titration, is found to be about 137, which compares excellently with the calculated value of about 134.

EXAMPLE IV Trisodium n-tetradecylaminodi(methylphosphonate), C H N[CH PO(ONa) [CH PO(ONa)(OH)], is prepared by dissolving 20 grams of free acid obtained in Example III in about 50 ml. of 10% NaOH solution and evaporating the aqueous solution to dryness at about 140 C. with the anhydrous form of the salt being formed.

EXAMPLE V Into a mixing vessel similar to that described in Example I above, are charged 164 parts of orthophosphorous acid, 266 parts of oleylamine, and 50 parts of water. The resulting mixture is stirred continuously through the remainder of the precess described below. The mixture is heated to 95 C., and maintained at about 95 C. while, over a period of about 20 minutes, 66 parts (10% excess) of paraformaldehyde are added slowly thereinto. Then for an additional hour after all formaldehyde has been added, the resulting mixture is refluxed at a temperature of about 110 C. after which the reaction mixture is cooled to room temperature. By nuclear magnetic resonance measurements, it is found that more than 90% of the orthophosphorous acid has been converted to the desired product, oleylaminodi(methylphosphonic acid), n-C H N(CH PO(OH) The equivalent weight of this product, by titration, is found to be about 158.2, which compares excellently with the calculated value of about 152.5.

EXAMPLE VI Into a mixing vessel similar to that described in Example I, above, are charged 134 parts of cyclohexylamine hydrochloride, 164 parts of orthophosphorous acid, and 25 parts of water. The resulting mixture is blended together and heated to 100 C. Then, over a period of about 30 minutes, 215 parts of benzaldehyde are slowly poured into the hot mixture. The temperature of the reaction mixture is maintained at about 100 C. for 2 hours, and then cooled to room temperature. Nuclear magnetic resonance analysis of the resulting product indicates that practically all of the orthophosphorous acid has been reacted to form the desired stable PCNC--P linkage. The equivalent weight of the resulting product, cyclohexyl aminodi(benzylidenephosphonic acid),

EXAMPLE VII Into a mixing vessel similar to that described in Example I, above, are charged 164 parts of orthophosphorous acid, 108 parts of benzylamine and 75.6 parts of concentrated HCl. The resulting mixture is stirred and heated at 100 C. while 120 parts of 37% aqueous formaldehyde solution excess) are added in the course of 3060 minutes. The solution is then kept at 90100 C. for about 2 to 3 hours. On cooling to room temperature benzylamino-di(methylphosphonic acid), C H CH N(CH PO(OH) precipitates with a yield of 85.7%. The equivalent weight of this product, by titration, is found to be about 102 which compares with the calculated value of about 98.4.

EXAMPLE VIII Into a conventional mixing vessel fitted with a reflux condenser are blended 119 parts of 'y-hydroxy-decylphosphonic acid and 58 parts of decylamine. The mixture is heated at about C. for about 3 hours. The resulting product, decylaminodi(nonylmethylphosphonic acid), C H N[CH(C H )PO(OI-I) precipitated in the form of its tri(decylamrnonium) salt upon cooling. The free acid is generated by prolonged grinding of the product in 5 N HCl followed by dilution of boiling water.

EXAMPLE IX EXAMPLE X Into a conventional 3-necked, 3-liter flask fitted with a reflux condenser, stirrer and thermometer were charged 426 parts of tetradecylamine, 485 parts of diethyl phoszphonate and 325 parts of 36% aqueous formaldehyde solution. The mixture is heated to about 70 C. at which temperature the reaction became exothermic with the temperature rising to about 120 C. The flask is allowed to cool to room temperature and the reaction product extracted with benzene. The solvent was separated from the oily product by distillation. This product, tetraethyl tetra decylaminodi (methylphosphonate) had a n.m.r. chemical shift of 24.9 ppm. The single n.m.r. peak of the product indicates the presence of only one type of phosphorous compound, i.e., tetraethyl tetradecyl aminodi (methylphosphonate) EXAMPLE XI A ketimine is prepared from 182 parts of n-hexylamine and 105 parts of acetone by reacting the acetone with the primary amine in the presence of anhydrous potassium carbonate, separating the ketimine from the aqueous layer and drying thoroughly over potassium hydroxide. This procedure resulted in 231 parts of the ketimine.

Into a reaction vessel similar to that described in Example X are charged the 231 parts of the ketimine and 226 parts of diethyl phosphonate. The mixture is heated to 50 C. at which temperature the reaction is initiated as indicated by the rise in temperature to about 120 C. After cooling to room temperature the resulting product is treated with 50 parts of paraformaldehyde and 225 parts of diethyl phosphonate. This mixture is heated under stirring to about 90 C. at which temperature a vigorous reaction takes place as indicated by the dissolution of the solid paraformaldehyde and an increase of the temperature to 110 C. The resulting product is tetraethyl n-hexyl amino(isopropylidene phosphonate) (methyl phosphonate),

An imine is prepared by reacting 144 parts of butyraldehyde with 214 parts of benzylamine in the presence of anhydrous potassium carbonate, separating the imine product from the aqueous layer and drying over potassium hydroxide. This procedure resulted in a quantity of 308 parts of the imine.

Into a reaction vessel similar to that described in Example X are charged 260 parts of diethyl phosphonate and the 308 parts of imine. 50 C. to initiate the reaction. After cooling to room temperature the resulting product is further reacted with 60 parts of paraformaldehyde and 260 parts of diethyl phosphonate by heating to about 90 C. under stirring, at which temperature a vigorous reaction occurs with the desired product, tetraethyl benzylamino(butylidene phosphonate) (methyl phosphonate),

Compounds representative of the instant invention a which can be prepared by methods such as those described in .the foregoing examples are:

(1) Long chain aliphatic hydrocarbyl-amino-di-alkylene phosphorus compounds, such as The mixture is heated to about C4H9N (C Hs O) 2) 2, n-butyl-amin0dibenzylidene phosphonic acid) 12 24 9 19) 2)2, Y Y- dode cane-amino-di nonyl methyl phosphonic acid) C H N [C (CH P0 (OH) [CH PO (OH) dodecylamino (isopropylidene phosphonic acid) (methyl phosphonic acid) decyl-amino cyclohexyl methyl phosphonic acid) (methyl phosphonic acid) 12 25 10 'I) )2] 2 )2] decyl-amino(1-naphthyl methyl phosphonic acid) (methyl phosphonic acid) nC H N CH P (0) (0 0a dicalcium-n-butyl-amino di (methyl phosphonate) 12 25 2 ON 3 4) 2] 2 3 4) (OH) tri-tetramethyl ammonium dodecyl-amino-di- (methyl phosphonate) (O NH CH CH OH) (OH) 1, tri-ethanol ammonium dodecyl-amino-di(methyl phosphonate) 14 29 2 4 2] H2 (ONH4) tri-ammonium tetradecyl-amino-di(methyl phosphonate) C H N (CH PO (OCH C H tetrahenzyl-n-hexylamino-di (methyl phosphonate) C6H13N 2) 2, tetraphenylethyln-hexyl-amino-di(methyl phosphonate) (2) Monocyclic, alicyclic-amino-di-alkylene phosphorus compounds, such as C H N CH PO (OH 2 cyclobutyl-amino-di (methyl phosphonic acid) OHC H N (CH PO (OH 2 Z-hydroxy-cyclohexylamino-di (methyl phosphonic acid) C H N( CH PO (OH) cyclopentyl-amino-di( methyl phosphonic acid) C H N C (CH P0 (OH) 2 cycIopentyLaminQ-di- (isoprozpylidene phosphonic acid) C H N (CH PO (OC H tetraphenyl-cyclohexylamino-di(methyl phosphonate) (3) Monocyclic, aryl-amino-di-alkylene phosphorus compounds, such as C H N (CH PO (OH) 2 phenyl-amino-di methyl phosph onic acid) C H N [C CH P0 (OH [CH PO (OH) phenylamino(isopropylidene phosphonic acid) (methyl phosphonic acid) (N0 C H N(CH PO (OH) 2,4-dinitro-phenylamino-di (methyl phosphonic acid) COOH (C 11 N (CH PO (OH) 4-carboxy-phenylamino-di (methyl phosphonic acid) (Cl 2 OH C H N(CH PO(OH) 2 3,5 dichloro-6- hydroxy-phenyl-amino-di (methyl phosphonic acid) OH) C H N CH PO( OH) 2 4-hydroxy-phenyl-aminodi (methyl phosphonic acid) C6H3N 2 2, 3-IlitI'O-4- methoxy-phenyl-amino-di (methyl phosphonic acid) C H N CH PO( OC H tetrahexyl-phenyl-aminodi (methyl phosphonate) C H N CH PO (OC H 2 tetra-l l-dodecene-phenylamino-di(methyl phosphonate) (4) Dicyclic, aryl-amino-di-alkylene phosphorus compounds, such as Cl C H (C H N CH PO(OH 4-chloro-4-N- drp'henyl-amino-di(methyl phosphonic acid) (OH) C H N(CH PO (OH) 4-hydroxy-naphthyl-1- a-mino-di(methyl phosphonic acid) (OH) (SO H) C H N(CH PO (OH) 1-sulfo-3- hydroxy-naphthyl-1-amino-di-(methyl phosphonic acid) (5) Monocyclic, alkaryl-amino-di-alkylene phosphorus compounds, such as (6) Dicyclic, alkaryl-amino-di-alkylene phosphorus compounds, such as (CH C1UH7N(CH2PO (OH) methyl-naphthyl-2- amino-di (methyl phosphonic acid) (CH3) cH N( 2 2, 2-methyl- 1- hydroxy-4-naphthyl-amino-di(methyl phosphonic acid) (C H) C H N(CH PO (OH) 7-dodecyl-naphthyl-2- amino-di( methyl phosphonic acid) (7) Monocyclic, aralkyl-amino-di-alkylene phosphorus compounds, such as C H CH CH N (CH PO( OH 2 phenylethyl-aminodi (methyl phosphonic acid) C H CH CH CH N(CH PO (OH) phenylpnopylamino-di (methyl phosphonic acid) phenylmethyl-arnino(Z-pyridyl methyl phosphonic acid) (methyl phosphonic acid) CgH CH CHgN (OH PO'( O Ca dicalcium-phenylethylamino-di (methyl phosphonate) (8) Monocyclic, N-containing heterocyclic-a-mino-dialkylene phosphorus compounds, such as,

C N=H N (CH PO( OH) 2-N-pyridyl-amino-di(methyl phosphonic acid) both of these properties to be effectively exhibited by the same compound. As can be appreciated, such compounds can advantageously be utilized in applications which can use the foregoing properties, such as, detergent compositions. In many detergent applications such as textile Washing and hard surface cleaning, the ability of the detergent oomposition to remove the soil and keep the soil suspended in the washing medium is of paramount importance.

The long chain hydrocarbyl-amino-di-lower alkylene phosphonic acids or the salts thereof are preferred in applications which use the combined surfactancy and defiocculating properties. These compounds are of the following formula:

YOORrRRaO OY I I YO R2 R4 OY wherein: R is selected from the class consisting of saturated and ethylenically unsaturated aliphatic hydrocarbyl radicals containing from 4 to 20 carbon atoms; R R R and R are selected from the class consisting of hydrogen and lower alkyl groups (1 to 4 carbon atoms); and Y is a cation. By the term cation is meant a hydrogen ion, alkali metal cation, alkaline earth metal cation, ammonium ion, or an amine ion.

As used in detergent compositions, the compounds of the instant invention are preferably formulated with other components, i.e., builders such as sodium tripolyphosphate, anti-redeposition agents such as carboxymethyl cellulose, brightening agents and the like, in amounts between about 10% to by weight of the detergent composition.

Compounds illustrative of the invention were tested for surfactancy properties by determining surface tension measurements with a Du Nuoy Tensiometer in distilled water at room temperature. The compounds tested were at concentrations believed representative of detergent concentrations used in actual applications. The results of the test are tabulated below.

Table 1 Surface Tension (dyne/cm) at indicated molar con- Cornpound centrations (10) Water ylphosphonate phosphonaten -amino-di-methylphosphonate meth phosphonate phosphonate ylphos honate phosphonate (11) Sodium dodecylbenzene sulfonate As can be observed from the above table compounds illustrative of the invention, i.e., (2), (3), (4), (5), (6), (7), (8), and (9) all exhibit the ability to lower the surface tension of water (10). Compounds (5), (6), (7), and 8) all compared very favorably with sodium dodecylbenzene sulfonate (11) a widely used surfactant. It should be noted that compound 1) exhibited no appreciable ability to lower the surface tension of water. As can be appreciated, therefore, by reason of their surfactancy compounds of this invention are particularly well suited for use in detergent compositions.

Compounds illustrative of the invention were tested for deflocculating properties in a carefully controlled kaolin slurry. The kaolin used in the evaluation was essentially free of impurities and was placed in an aqueous slurry with a solids content about 68%. The slurry throughout the evaluation was maintained at a pH of about 7 with NaOH. The apparent viscosity was determined with a Stormer viscometer at 300 r.p.m. The results of the tests are tabulated below.

Table 2 and water were found to completely dissolve one volume of hexane.

B. A solution of equal volumes of tetraethyl iso-isobutyl amino di-methylphosphonate,

and water were found to completely dissolve one-half a volume of hexane.

Apparent Viscosity (cp.) at 300 v.p.m. Stormer at indicated weight percent of defiocculated on a dry clay basis As can be observed from the above table, minor amounts of the compounds illustrative of the invention, i.e., (2), (3), (4), (5) and (6), deflocculated a plastic slurry into a flowable slurry. In addition, compounds (2), (3) and (4) compared very favorably with sodium tripolyphosphate (7), a widely used deflocculant, and compound (1).

The esters of organo-amino-di-alkylene phosphonic acids were found not only to be completely miscible with water but also highly soluble in organic solvents, such as hydrocarbon solvent, i.e., hexane and pentane, carbon tetra chloride, haloethylene solvents, i.e., perchloroethylene, ethers, alcohols, and the like. Also, the esters were found to impart a solubilizing action to water in waterimmiscible solvents, such as many of the previously mentioned solvents. This totally unexpected property renders them highly useful as gasoline de-icer additives and along with their surfactancy properties render them useful as dry cleaning detergents. As can be appreciated, however, the unique ability to impart a solubilizing action to water in water-immiscible solvents can be utilized in many and varied applications and therefore, the foregoing mentioned applications are merely indicative of their use.

The esters of long chain hydrocarbyl-amino-di-lower alkylene phosphonic acids are preferred in applications which use the combined surfactancy and/or water solubilizing properties. These compounds are of the following formula:

wherein: R is selected from the class consisting of saturated and ethylenically unsaturated aliphatic hydrocarbyl radicals containing from 4 to carbon atoms; R R R and R are selected from the group consisting of hydrogen and lower alkyl groups (1 to 4 carbon atoms); and R is selected from the class consisting of alkyl groups of from 1 to 20 carbon atoms, aryl group-s and alkylaryl groups.

Because of the complexity of the ternary solubility diagram of the esters of the instant invention-waterwater-immiscible solvents the following is set forth for example purposes only.

A. A solution of equal volumes of tetraethyl tetradecylamino-di-methylphosphonate,

H2O Added Compound (grams) (1) tetraethyl hexadecylaminodimethylphosphonate 3 C1uHasN( z 2 5)z)z (2) tetraethyl tetradecyl amino-dimethy1phosphonate 1 C12 25N( 2 2H5)2)2 (3) tetraethyl octylaminodimethylphosphonate 7 (4) tetraethyl iso-butyl amino-dimethylphosphonate Several drops lSO-C4H9N (CHzPO (0 02115) 2):

It should be noted that the foregoing example solutions exhibited no phase separation at the end of a one week period of standing nor was there a phase separation after the solutions had been centrifuged at 5,000 r.p.m. for one hour indicating that the water was completely dissolved in the water-immiscible solvent. It should further be noted that tetraethyl methyl amino-di-methyl phosphonate, CH N(CH PO(OC H did not impart a solubi'lizing action to water in a water-immiscible solvent.

As previously mentioned the ester compounds of the instant invention are useful in gasoline de-icer additives and are preferably used in amounts of from .005 to .1% by weight. And advantageous feature of these de-icer additives, by reason of their phosphorus content, is their ability to function either wholly as the primary additive for surface ignition control or in conjunction with other known phosphorus additives for surface ignition control.

As dry cleaning additives the ester compounds of the instant invention can be used as either the primary surfactant or in conjunction with other surfactants. When used as substantially the primary surfactant with many of the common organic solvents, such as, Stoddards solvent and perchloroethylene, amounts within the range of .05 to 4% by weight are rusually sufiicient with amounts about 2% by weight being preferre'd.

Although the compounds of the instant invention as W611 as their uses have been described with a degree of particularity, the invention herein is intended to be limited only by the claims set forth hereinafter.

What is claimed is:

1. A gasoline composition containing an ester of an organo-amino-di-alkylene phosphonic acid in amounts of from 0.005 to 0.1% by weight of said composition, said ester having the formula wherein R is selected from a class consisting of aliphatic hydrocarbyl groups containing from 4 to 30 carbon atoms, alicyclic groups containing from 4 to 6 carbon atoms, aryl groups containing from 6 to 10 carbon atoms, alkaryl groups containing from 7 to 30 carbon atoms and aralkyl groups containing from 7 to 30 carbon atoms; R R R and R are selected from the class consisting of hydrogen, aliphatic hydrocarbyl groups containing from 1 to 30 carbon atoms, alicyclic groups containing from 4 to 6 carbon atoms, aryl groups containing from 6 to 10 carbon atoms, alkaryl groups containing from 7 to 30 carbon atoms and aralkyl groups containing from 7 to 30 carbon atoms; and X is selected from the group consisting of alkyl groups of cfrom 1 to 30 carbon atoms, phenyl, benzyl and phenylethyl.

2. A gasoline composition containing an ester of longchain hydrocarbyl-amino-di-lower alkylene phosphonic acids in amounts of from 0.005 to 0.1% by weight of said composition, said ester having the formula wherein R is selected from the class consisting of saturated and ethylenically unsaturated aliphatic hydrocarbyl radicals containing from 4 to 20 carbon atoms; R R R and R have the structure C H wherein x is an integer from 0 to 4 inclusive; and R is selected from the group consisting of alkyl groups of from 1 to 20 carbon atoms.

3. The gasoline composition of claim 2, wherein said ester is tetraethyl tetradecyl amino-di-methylphosponate.

4. The gasoline composition of claim 2, wherein said ester is tetraethyl hexadecylamino-di-methylphosphon ate.

5. The gasoline composition of claim 2, wherein said ester is tetraethyl octylaminodi-methylphosphonate.

6. The gasoline composition of claim 2, wherein said ester is tetraethyl isoabutyl amino-di-\methylphosphonate. 

1. A GASOLINE COMPOSITION CONTAINING AN ESTER OF AN ORGANO-AMINO-DI-ALKYLENE PHOSPHONIC ACID IN AMOUNTS OF FROM 0.005 TO 0.1% BY WEIGHT OF SAID COMPOSITION, SAID ESTER HAVING THE FORMULA 